Replication Stress Induces Genome-wide Copy Number Changes in Human Cells that Resemble Polymorphic and Pathogenic Variants
- 19 February 2009
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 84 (3), 339-350
- https://doi.org/10.1016/j.ajhg.2009.01.024
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (CA43222)
This publication has 50 references indexed in Scilit:
- Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancersProceedings of the National Academy of Sciences of the United States of America, 2008
- 53BP1 facilitates long-range DNA end-joining during V(D)J recombinationNature, 2008
- 53BP1 promotes non-homologous end joining of telomeres by increasing chromatin mobilityNature, 2008
- Mapping and sequencing of structural variation from eight human genomesNature, 2008
- Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencingNature Genetics, 2008
- The Fine-Scale and Complex Architecture of Human Copy-Number VariationAmerican Journal of Human Genetics, 2008
- Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation ProfilesAmerican Journal of Human Genetics, 2008
- Replication stress induces tumor-like microdeletions in FHIT /FRA3BProceedings of the National Academy of Sciences of the United States of America, 2008
- Global variation in copy number in the human genomeNature, 2006
- A high-resolution survey of deletion polymorphism in the human genomeNature Genetics, 2005